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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1989 | 1 |
2006 | 1 |
2007 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
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Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy.
Atherosclerosis. 2013 Apr;227(2):342-8. doi: 10.1016/j.atherosclerosis.2013.01.007. Epub 2013 Jan 19.
Atherosclerosis. 2013.
PMID: 23375686
Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.
Soria LF, Ludwig EH, Clarke HR, Vega GL, Grundy SM, McCarthy BJ.
Soria LF, et al.
Proc Natl Acad Sci U S A. 1989 Jan;86(2):587-91. doi: 10.1073/pnas.86.2.587.
Proc Natl Acad Sci U S A. 1989.
PMID: 2563166
Free PMC article.
Item in Clipboard
Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations.
Futema M, Plagnol V, Li K, Whittall RA, Neil HA, Seed M; Simon Broome Consortium; Bertolini S, Calandra S, Descamps OS, Graham CA, Hegele RA, Karpe F, Durst R, Leitersdorf E, Lench N, Nair DR, Soran H, Van Bockxmeer FM; UK10K Consortium; Humphries SE.
Futema M, et al.
J Med Genet. 2014 Aug;51(8):537-44. doi: 10.1136/jmedgenet-2014-102405. Epub 2014 Jul 1.
J Med Genet. 2014.
PMID: 24987033
Free PMC article.
Item in Clipboard
ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature.
Sabbagh AS, Daher RT, Otrock ZK, Khalek RN, Zaatari GS, Mahfouz RA.
Sabbagh AS, et al.
Mol Biol Rep. 2007 Dec;34(4):267-70. doi: 10.1007/s11033-006-9041-7. Epub 2006 Dec 8.
Mol Biol Rep. 2007.
PMID: 17160438
Review.
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